WO2014011911A3 - Irak inhibitors and uses thereof - Google Patents
Irak inhibitors and uses thereof Download PDFInfo
- Publication number
- WO2014011911A3 WO2014011911A3 PCT/US2013/050120 US2013050120W WO2014011911A3 WO 2014011911 A3 WO2014011911 A3 WO 2014011911A3 US 2013050120 W US2013050120 W US 2013050120W WO 2014011911 A3 WO2014011911 A3 WO 2014011911A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- irak inhibitors
- irak
- inhibitors
- furano
- pyrrolo
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
- C07D491/044—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
- C07D491/048—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being five-membered
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
The present invention provides furano- and pyrrolo- pyrimidine and pyridine compounds, compositions thereof, and methods of using the same.
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201261670386P | 2012-07-11 | 2012-07-11 | |
| US61/670,386 | 2012-07-11 | ||
| US201261682616P | 2012-08-13 | 2012-08-13 | |
| US61/682,616 | 2012-08-13 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| WO2014011911A2 WO2014011911A2 (en) | 2014-01-16 |
| WO2014011911A3 true WO2014011911A3 (en) | 2015-07-16 |
Family
ID=49914495
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/US2013/050120 Ceased WO2014011911A2 (en) | 2012-07-11 | 2013-07-11 | Irak inhibitors and uses thereof |
Country Status (2)
| Country | Link |
|---|---|
| US (1) | US20140018361A1 (en) |
| WO (1) | WO2014011911A2 (en) |
Families Citing this family (65)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2012097013A1 (en) | 2011-01-10 | 2012-07-19 | Nimbus Iris, Inc. | Irak inhibitors and uses thereof |
| WO2012178125A1 (en) | 2011-06-22 | 2012-12-27 | Vertex Pharmaceuticals Incorporated | Compounds useful as inhibitors of atr kinase |
| TW201728592A (en) | 2012-01-10 | 2017-08-16 | 林伯士艾瑞斯公司 | IRAK inhibitors and uses thereof |
| US9085586B2 (en) | 2012-07-11 | 2015-07-21 | Nimbus Iris, Inc. | IRAK inhibitors and uses thereof |
| WO2014011906A2 (en) | 2012-07-11 | 2014-01-16 | Nimbus Iris, Inc. | Irak inhibitors and uses thereof |
| CN107501275B (en) | 2012-12-07 | 2019-11-22 | 沃泰克斯药物股份有限公司 | It can be used as the compound of ATR kinase inhibitor |
| EP2943202A4 (en) | 2013-01-10 | 2016-08-24 | Nimbus Iris Inc | Irak inhibitors and uses thereof |
| US8778365B1 (en) | 2013-01-31 | 2014-07-15 | Merz Pharmaceuticals, Llc | Topical compositions and methods for making and using same |
| PE20151764A1 (en) | 2013-02-22 | 2015-12-03 | Pfizer | DERIVATIVES OF PIRROLO [2,3-D] PYRIMIDINE |
| US9663519B2 (en) | 2013-03-15 | 2017-05-30 | Vertex Pharmaceuticals Incorporated | Compounds useful as inhibitors of ATR kinase |
| JP6426694B2 (en) | 2013-03-15 | 2018-11-21 | グローバル ブラッド セラピューティクス インコーポレイテッド | Compounds for the modification of hemoglobin and their use |
| EP2970288A1 (en) | 2013-03-15 | 2016-01-20 | Vertex Pharmaceuticals Incorporated | Compounds useful as inhibitors of atr kinase |
| JP2016512239A (en) | 2013-03-15 | 2016-04-25 | バーテックス ファーマシューティカルズ インコーポレイテッドVertex Pharmaceuticals Incorporated | Compounds useful as inhibitors of ATR kinase |
| CA2925211A1 (en) | 2013-09-27 | 2015-04-02 | Nimbus Iris, Inc. | Irak inhibitors and uses thereof |
| EA202092627A1 (en) | 2013-11-18 | 2021-09-30 | Глобал Блад Терапьютикс, Инк. | COMPOUNDS AND THEIR APPLICATIONS FOR HEMOGLOBIN MODULATION |
| PT3077397T (en) | 2013-12-06 | 2020-01-22 | Vertex Pharma | 2-amino-6-fluoro-n-[5-fluoro-pyridin-3-yl]pyrazolo[1,5-a]pyrimidin-3-carboxamide compound useful as atr kinase inhibitor, its preparation, different solid forms and radiolabelled derivatives thereof |
| WO2015164374A1 (en) * | 2014-04-22 | 2015-10-29 | Nimbus Iris, Inc. | Irak inhibitors and uses thereof |
| JP6568111B2 (en) | 2014-06-05 | 2019-08-28 | バーテックス ファーマシューティカルズ インコーポレイテッドVertex Pharmaceuticals Incorporated | Radiolabeled derivatives of 2-amino-6-fluoro-N- [5-fluoro-pyridin-3-yl] pyrazolo [1,5-a] pyrimidine-3-carboxamide compounds useful as ATR kinase inhibitors, Preparation of compounds and their different solid forms |
| HRP20191375T1 (en) | 2014-06-17 | 2019-11-01 | Vertex Pharma | Method for treating cancer using a combination of chk1 and atr inhibitors |
| GB201411236D0 (en) | 2014-06-25 | 2014-08-06 | Takeda Pharmaceutical | Novel compounds |
| KR102523430B1 (en) | 2014-08-04 | 2023-04-19 | 누에볼루션 에이/에스 | Optionally fused heterocyclyl-substituted derivatives of pyrimidine useful for the treatment of inflammatory, metabolic, oncologic and autoimmune diseases |
| ES2750655T3 (en) | 2014-08-12 | 2020-03-26 | Pfizer | Pyrrolo [2,3-d] pyrimidine derivatives useful to inhibit Janus kinase |
| EP3200788B1 (en) * | 2014-09-30 | 2019-09-18 | Merck Sharp & Dohme Corp. | Inhibitors of irak4 activity |
| CN114057765A (en) | 2015-02-02 | 2022-02-18 | 瓦洛健康股份有限公司 | 3-Aryl-4-amido-bicyclo[4,5,0]hydroxamic acids as HDAC inhibitors |
| AR103598A1 (en) | 2015-02-02 | 2017-05-24 | Forma Therapeutics Inc | BICYCLIC ACIDS [4,6,0] HYDROXAMICS AS HDAC INHIBITORS |
| WO2017004133A1 (en) * | 2015-06-29 | 2017-01-05 | Nimbus Iris, Inc. | Irak inhibitors and uses thereof |
| WO2017024589A1 (en) * | 2015-08-13 | 2017-02-16 | 北京韩美药品有限公司 | Irak4 inhibitor and use thereof |
| CN107531710B (en) * | 2015-08-13 | 2020-02-14 | 北京韩美药品有限公司 | IRAK4 inhibitor and application thereof |
| WO2017025849A1 (en) * | 2015-08-13 | 2017-02-16 | Pfizer Inc. | Bicyclic-fused heteroaryl or aryl compounds |
| RU2768621C1 (en) | 2015-09-30 | 2022-03-24 | Вертекс Фармасьютикалз Инкорпорейтед | Method of treating cancer using a combination of dna damaging agents and atr inhibitors |
| SG10201508795XA (en) * | 2015-10-23 | 2017-05-30 | Agency Science Tech & Res | Method for treating cancer |
| US9630968B1 (en) | 2015-12-23 | 2017-04-25 | Arqule, Inc. | Tetrahydropyranyl amino-pyrrolopyrimidinone and methods of use thereof |
| CN105461728A (en) * | 2015-12-29 | 2016-04-06 | 中山大学 | 4-substituted amino-6-methoxycarbonyl group benzofuran and [2,3-d] pyrimidine compound and preparing method |
| WO2017205762A1 (en) * | 2016-05-27 | 2017-11-30 | Pharmacyclics Llc | Inhibitors of interleukin-1 receptor-associated kinase |
| US10555935B2 (en) | 2016-06-17 | 2020-02-11 | Forma Therapeutics, Inc. | 2-spiro-5- and 6-hydroxamic acid indanes as HDAC inhibitors |
| JP2019530650A (en) | 2016-08-24 | 2019-10-24 | アークル インコーポレイテッド | Amino-pyrrolopyrimidinone compounds and methods of use thereof |
| AU2017388054B2 (en) | 2016-12-28 | 2022-03-24 | Dart Neuroscience, Llc | Substituted pyrazolopyrimidinone compounds as PDE2 inhibitors |
| JOP20180011A1 (en) | 2017-02-16 | 2019-01-30 | Gilead Sciences Inc | Perulo derivatives [1, 2-b] pyridazine |
| WO2019001461A1 (en) * | 2017-06-27 | 2019-01-03 | 南京明德新药研发股份有限公司 | INHIBITOR OF IRAQ4 |
| WO2019060693A1 (en) | 2017-09-22 | 2019-03-28 | Kymera Therapeutics, Inc. | Crbn ligands and uses thereof |
| MX2020003190A (en) | 2017-09-22 | 2020-11-11 | Kymera Therapeutics Inc | Protein degraders and uses thereof. |
| AU2018373258B2 (en) | 2017-11-27 | 2023-03-02 | Dart Neuroscience, Llc | Substituted furanopyrimidine compounds as PDE1 inhibitors |
| WO2019111218A1 (en) | 2017-12-08 | 2019-06-13 | Cadila Healthcare Limited | Novel heterocyclic compounds as irak4 inhibitors |
| IL315310A (en) | 2017-12-26 | 2024-10-01 | Kymera Therapeutics Inc | IRAK joints and used in them |
| US11485743B2 (en) | 2018-01-12 | 2022-11-01 | Kymera Therapeutics, Inc. | Protein degraders and uses thereof |
| US11512080B2 (en) | 2018-01-12 | 2022-11-29 | Kymera Therapeutics, Inc. | CRBN ligands and uses thereof |
| EP3817822A4 (en) | 2018-07-06 | 2022-07-27 | Kymera Therapeutics, Inc. | PROTEIN DEGRADING AGENTS AND THEIR USES |
| US11292792B2 (en) | 2018-07-06 | 2022-04-05 | Kymera Therapeutics, Inc. | Tricyclic CRBN ligands and uses thereof |
| TWI721483B (en) | 2018-07-13 | 2021-03-11 | 美商基利科學股份有限公司 | Pyrrolo[1,2-b]pyridazine derivatives |
| EP3886904A4 (en) | 2018-11-30 | 2022-07-13 | Kymera Therapeutics, Inc. | IRAQ-TYPE KINASE DEGRADING AGENTS AND THEIR USES |
| CN111662295B (en) * | 2019-03-05 | 2021-09-10 | 珠海宇繁生物科技有限责任公司 | IRAK4 kinase inhibitor and preparation method thereof |
| US11591332B2 (en) | 2019-12-17 | 2023-02-28 | Kymera Therapeutics, Inc. | IRAK degraders and uses thereof |
| EP4076520A4 (en) | 2019-12-17 | 2024-03-27 | Kymera Therapeutics, Inc. | IRAQ DEGRADATION AGENTS AND THEIR USES |
| US11447479B2 (en) | 2019-12-20 | 2022-09-20 | Nuevolution A/S | Compounds active towards nuclear receptors |
| PE20230240A1 (en) | 2019-12-20 | 2023-02-07 | Nuevolution As | ACTIVE COMPOUNDS AGAINST NUCLEAR RECEPTORS |
| EP4126875A1 (en) | 2020-03-31 | 2023-02-08 | Nuevolution A/S | Compounds active towards nuclear receptors |
| US11780843B2 (en) | 2020-03-31 | 2023-10-10 | Nuevolution A/S | Compounds active towards nuclear receptors |
| TW202210483A (en) | 2020-06-03 | 2022-03-16 | 美商凱麥拉醫療公司 | Crystalline forms of irak degraders |
| TW202241891A (en) | 2020-12-30 | 2022-11-01 | 美商凱麥拉醫療公司 | Irak degraders and uses thereof |
| CA3207049A1 (en) | 2021-02-15 | 2022-08-18 | Jared Gollob | Irak4 degraders and uses thereof |
| JP2024519215A (en) | 2021-05-07 | 2024-05-09 | カイメラ セラピューティクス, インコーポレイテッド | CDK2 degraders and their uses |
| TW202334165A (en) | 2021-10-29 | 2023-09-01 | 美商凱麥拉醫療公司 | Irak4 degraders and synthesis thereof |
| IL314437A (en) | 2022-01-31 | 2024-09-01 | Kymera Therapeutics Inc | Irak degraders and uses thereof |
| WO2024107393A1 (en) * | 2022-11-14 | 2024-05-23 | Schrödinger, Inc. | Tricyclic compounds |
| CN116731030A (en) * | 2023-06-07 | 2023-09-12 | 湖北医药学院 | Synthesis method and antitumor application of several furopyrimidine-ibuprofen hybrid derivatives |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6297238B1 (en) * | 1999-04-06 | 2001-10-02 | Basf Aktiengesellschaft | Therapeutic agents |
| US20100143341A1 (en) * | 2005-06-22 | 2010-06-10 | Develogen Aktiengesellschaft | Thienopyrimidines for pharmaceutical compositions |
| US8058285B2 (en) * | 2004-07-23 | 2011-11-15 | The Medicines Company (Leipzig) Gmbh | Substituted pyrido [3′, 2′: 4, 5] thieno [3, 2-D] pyrimidines and pyrido [3′, 2′: 4, 5] furo [3, 2-D] pyrimidines used as inhibitors of the PDE-4 and/or the release of TNF-ALPHA |
| WO2012007375A1 (en) * | 2010-07-13 | 2012-01-19 | F. Hoffmann-La Roche Ag | Pyrazolo [1, 5a] pyrimidine and thieno [3, 2b] pyrimidine derivatives as irak4 modulators |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6680322B2 (en) * | 1999-12-02 | 2004-01-20 | Osi Pharmaceuticals, Inc. | Compounds specific to adenosine A1 receptors and uses thereof |
-
2013
- 2013-07-11 US US13/939,832 patent/US20140018361A1/en not_active Abandoned
- 2013-07-11 WO PCT/US2013/050120 patent/WO2014011911A2/en not_active Ceased
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6297238B1 (en) * | 1999-04-06 | 2001-10-02 | Basf Aktiengesellschaft | Therapeutic agents |
| US8058285B2 (en) * | 2004-07-23 | 2011-11-15 | The Medicines Company (Leipzig) Gmbh | Substituted pyrido [3′, 2′: 4, 5] thieno [3, 2-D] pyrimidines and pyrido [3′, 2′: 4, 5] furo [3, 2-D] pyrimidines used as inhibitors of the PDE-4 and/or the release of TNF-ALPHA |
| US20100143341A1 (en) * | 2005-06-22 | 2010-06-10 | Develogen Aktiengesellschaft | Thienopyrimidines for pharmaceutical compositions |
| WO2012007375A1 (en) * | 2010-07-13 | 2012-01-19 | F. Hoffmann-La Roche Ag | Pyrazolo [1, 5a] pyrimidine and thieno [3, 2b] pyrimidine derivatives as irak4 modulators |
Non-Patent Citations (2)
| Title |
|---|
| NGO, VN ET AL.: "Oncogenically active MYD88 mutations in human lymphoma.", NATURE, vol. 470, no. 7332, 22 December 2010 (2010-12-22), pages 115 - 119, Retrieved from the Internet <URL:http://www.ncbi.nlm.nih.gov/pubmed/21179087> [retrieved on 20131129] * |
| SONG, KW ET AL.: "The kinase activities of Interleukin-1 receptor associated kinase ( IRAK )-1 and 4 are redundant in the control of Inflammatory cytokine expression in human cells.", MOL IMMUNOL, vol. 46, no. 7, 31 January 2009 (2009-01-31), pages 1458 - 1466, Retrieved from the Internet <URL:http://www.ncbi.nim.nih.gov/pubmed/19161383> [retrieved on 20131129] * |
Also Published As
| Publication number | Publication date |
|---|---|
| US20140018361A1 (en) | 2014-01-16 |
| WO2014011911A2 (en) | 2014-01-16 |
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